Person who experienced the adverse event (patient)
Event ID | CASEID | CASEVERSION | I F COD | EVENT DT | MFR DT | INIT FDA DT | FDA DT | REPT COD | AUTH NUM | MFR NUM | MFR SNDR | LIT REF | AGE | AGE COD | AGE GRP | GNDR COD | E SUB | WT | WT COD | REPT DT | TO MFR | OCCP COD | REPORTER COUNTRY | OCCR COUNTRY |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125658171 | 12565817 | 1 | I | 2014 | 20160711 | 20160718 | 20160718 | EXP | PHHY2016BR097032 | NOVARTIS | 0.00 | F | Y | 80.00000 | KG | 20160718 | MD | BR | BR |
Drug(s) used by person
Event ID | CASEID | DRUG SEQ | ROLE COD | DRUGNAME | PROD AI | VAL VBM | ROUTE | DOSE VBM | CUM DOSE CHR | CUM DOSE UNIT | DECHAL | RECHAL | LOT NUM | EXP DT | NDA NUM | DOSE AMT | DOSE UNIT | DOSE FORM | DOSE FREQ |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
125658171 | 12565817 | 1 | PS | DIOVAN | VALSARTAN | 1 | Oral | 1 DF, QD | U | 21283 | 1 | DF | TABLET | QD |
Indications of drugs used
Event ID | CASEID | INDI DRUG SEQ | INDI PT |
---|---|---|---|
125658171 | 12565817 | 1 | Hypertension |
Outcome of event
Event ID | CASEID | OUTC COD |
---|---|---|
125658171 | 12565817 | OT |
Reactions reported
Event ID | CASEID | DRUG REC ACT | PT |
---|---|---|---|
125658171 | 12565817 | Alopecia | |
125658171 | 12565817 | Depressed mood | |
125658171 | 12565817 | Haemorrhage | |
125658171 | 12565817 | Malaise | |
125658171 | 12565817 | Metastatic malignant melanoma |
Reporting Sources (this data is often not reported and may therefore be missing here)
no results found |
Therapies reported
no results found |